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Overall Effectiveness Evaluation of the Blood Pressure Monitor

Overall Effectiveness Evaluation of the Blood Pressure Monitor

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108415
Enrollment
Unknown
Registered
2025-08-29
Start date
2025-09-05
Completion date
Unknown
Last updated
2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None

Interventions

Experimental group:Using a self-controlled design, each participant serves as their own control. Blood pressure is measured using a device with three cuffs, and at least three sets of valid blood pres

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Age > 12 years and gender is not limited; 2. Arm circumference of 15cm to 54cm (including the cut-off); 3. Voluntarily participate in blood pressure measurement and sign the informed consent form; 4. Be able to communicate well with the investigators, have good compliance, and follow the requirements of clinical research.

Exclusion criteria

Exclusion criteria: 1.Patients with implanted, electrical devices, such as cardiac pacemakers, defifibrillators; 2. Pregnant women (including patients with preeclampsia); 3. Individuals allergic to polyester, nylon, or plastic; 4. Patients with other conditions that may affect blood pressure measurement readings, such as atrial fibrillation, diabetes, etc.; 5. A subject is used repeatedly in a clinical investigation; 6. Persons with impaired consciousness cannot be adequately informed; 7.Other reasons that the investigators consider the person is not eligible for the research.

Design outcomes

Primary

MeasureTime frame
Mean difference and standard deviation of systolic-diastolic pressure difference;Standard deviation of the mean systolic and diastolic blood pressure;

Countries

China

Contacts

Public ContactZhang Li

Hebei General Hospital

1136329347@qq.com+86 132 4934 6346

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026